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Molecular Cytogenetics|August 4, 2017
Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunctionSandra Chantot-Bastaraud, Svea Stratmann, Frédéric Brioude, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 26, 2020
Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is importantThomas Eggermann, Johanna Brück, Cordula Knopp, et al.
Molecular Genetics & Genomic Medicine|November 28, 2017
The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Thomas Eggermann, Barbara Oehl-Jaschkowitz, Severin Dicks, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|July 13, 2005
Computer-assisted screw insertion into the first sacral vertebra using a three-dimensional image intensifier: results of a controlled experimental investigationD Briem, W Linhart, W Lehmann, et al.
European Radiology|April 21, 2006
Characterization of the peri-infarction zone using T2-weighted MRI and delayed-enhancement MRI in patients with acute myocardial infarctionAlexander Stork, Gunnar K Lund, Kai Muellerleile, et al.
Clinical Epigenetics|April 30, 2025
Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver-Russell phenotypeMatthias Begemann, Anna Lengyel, Eva Pinti, et al.
European Radiology|April 13, 2007
Multidetector CT urography: experimental analysis of radiation dose reduction in an animal modelJoern Kemper, Marc Regier, Paul M Bansmann, et al.
Pflugers Archiv : European Journal of Physiology|May 2, 2013
Regulation of ClC-2 gating by intracellular ATPGabriel Stölting, Georgeta Teodorescu, Birgit Begemann, et al.
Molecular Psychiatry|December 7, 2016
OTTO: a new strategy to extract mental disease-relevant combinations of GWAS hits from individualsH Ehrenreich, M Mitjans, S Van der Auwera, et al.
Molecular Genetics & Genomic Medicine|November 6, 2018
Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contracturesMiriam Elbracht, Florian Kraft, Matthias Begemann, et al.
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